about
Human genetics and genomics a decade after the release of the draft sequence of the human genomeEvolutionary dynamics of copy number variation in pig genomes in the context of adaptation and domesticationSeparating the wheat from the chaff: mitigating the effects of noise in a plastome phylogenomic data set from Pinus L. (Pinaceae)Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectivesA new chromosomal phylogeny supports the repeated origin of vectorial capacity in malaria mosquitoes of the Anopheles gambiae complexLUMPY: a probabilistic framework for structural variant discovery.Repetitive DNA and next-generation sequencing: computational challenges and solutionsUsing ERDS to infer copy-number variants in high-coverage genomesPrecision editing of large animal genomesThe Evolving Diagnostic and Genetic Landscapes of Autism Spectrum DisorderMechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome RearrangementsTransposable element detection from whole genome sequence dataImage processing for optical mappingIntegrating genetics and epigenetics in breast cancer: biological insights, experimental, computational methods and therapeutic potentialBest practices for evaluating single nucleotide variant calling methods for microbial genomicsSomatic mosaicism in the human genomeDevelopments in our understanding of the genetic basis of birth defectsComplexity of gene expression evolution after duplication: protein dosage rebalancingIntegrated analysis of whole-genome paired-end and mate-pair sequencing data for identifying genomic structural variations in multiple myelomaMassively parallel sequencing: the new frontier of hematologic genomicsMicroarray resources for genetic and genomic studies in chicken: a reviewA genetic model for neurodevelopmental diseaseComputational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challengesStructural variation discovery in the cancer genome using next generation sequencing: computational solutions and perspectivesUsing familial information for variant filtering in high-throughput sequencing studiesGene duplication as a mechanism of genomic adaptation to a changing environmentCNVs: harbingers of a rare variant revolution in psychiatric geneticsNew genes contribute to genetic and phenotypic novelties in human evolutionHigh throughput sequencing approaches to mutation discovery in the mouseConnecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 MiceWhole-Genome Sequencing of Native Sheep Provides Insights into Rapid Adaptations to Extreme Environments.Genome-Wide Detection of CNVs and Their Association with Meat Tenderness in Nelore CattleNew insights into the generation and role of de novo mutations in health and diseaseDetection of Genomic Structural Variants from Next-Generation Sequencing DataAppraisal of the technologies and review of the genomic landscape of ductal carcinoma in situ of the breastSCALCE: boosting sequence compression algorithms using locally consistent encodingPeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing dataPostzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individualsWinHAP: an efficient haplotype phasing algorithm based on scalable sliding windowsEstimating genomic diversity and population differentiation - an empirical comparison of microsatellite and SNP variation in Arabidopsis halleri
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description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Genome structural variation discovery and genotyping
@en
Genome structural variation discovery and genotyping.
@nl
type
label
Genome structural variation discovery and genotyping
@en
Genome structural variation discovery and genotyping.
@nl
prefLabel
Genome structural variation discovery and genotyping
@en
Genome structural variation discovery and genotyping.
@nl
P2860
P356
P1476
Genome structural variation discovery and genotyping
@en
P2093
Bradley P Coe
Evan E Eichler
P2860
P2888
P304
P356
10.1038/NRG2958
P50
P577
2011-03-01T00:00:00Z